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rs730880575

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880575(A;A)
Make rs730880575(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351437
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880575
ebirs730880575
HLIrs730880575
Exacrs730880575
Varsomers730880575
Maprs730880575
PheGenIrs730880575
hapmaprs730880575
1000 genomesrs730880575
hgdprs730880575
ensemblrs730880575
gopubmedrs730880575
geneviewrs730880575
scholarrs730880575
googlers730880575
pharmgkbrs730880575
gwascentralrs730880575
openSNPrs730880575
23andMers730880575
23andMe allrs730880575
SNP Nexus

SNPshotrs730880575
SNPdbers730880575
MSV3drs730880575
GWAS Ctlgrs730880575
Max Magnitude0
ClinVar
Risk rs730880575(A,C;A,C)
Alt rs730880575(A,C;A,C)
Reference rs730880575(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47372988C>T
CLNSRC
CLNACC RCV000223809.1,